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4-Hydroxy-4-phenyl-4H-naphthalen-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

120413-65-2

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120413-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120413-65-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,4,1 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120413-65:
(8*1)+(7*2)+(6*0)+(5*4)+(4*1)+(3*3)+(2*6)+(1*5)=72
72 % 10 = 2
So 120413-65-2 is a valid CAS Registry Number.

120413-65-2Relevant academic research and scientific papers

Method for selectively preparing hydroquinone monoether compound or quinol compound (by machine translation)

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Paragraph 0040-0045; 0117-0119; 0154-0155, (2020/12/30)

The method comprises the following steps: taking an organic boric acid compound and a p-benzoquinone compound as a reaction raw material, under the action of a copper catalyst, selectively reacting to obtain a hydroquinone monoether compound or a quinol compound. Compared with the prior art, the method disclosed by the invention adopts a one-pot reaction, can selectively obtain two products through solvent control, is suitable for preparing various types of hydroquinone monoether compounds and quinol compounds, and has wide applicability. The substrate functional group is high in tolerance and wide in substrate range. The raw material and the catalyst are cheap and easily available, the reaction conditions are mild, the reaction solvent is green and environment-friendly, the post-treatment is simple, and the yield and purity of the product are high. The preparation method is convenient. The method is rapid and efficient, and has a good application prospect in drug molecule synthesis. (by machine translation)

Competitive Dienone-Phenol Type Rearrangements for the Regioselective Preparation of 2,4-Disubstituted-Naphth-1-ols

Dodge, Jeffrey A.,Chamberlin, A. Richard

, p. 4827 - 4830 (2007/10/02)

The regioselective preparation of 2,4-substituted-naphth-1-ols via a variant of the dienone-phenol rearrangement is described.

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